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FDA 510(k)

JOBST ATHROMBIC PUMP SYSTEM 2100

K-Number: K963929 · 1997-01-27

Decision Date1997-01-27
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JOBST ATHROMBIC PUMP SYSTEM 2100 is the device name listed in this FDA 510(k) record. The listed applicant is Jobst A Beiersdorf Co.. It received FDA 510(k) clearance on 1997-01-27 under 510(k) number K963929. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOBST ATHROMBIC PUMP SYSTEM 2100?

JOBST ATHROMBIC PUMP SYSTEM 2100 is a medical device that received FDA 510(k) clearance on 1997-01-27. The listed applicant is Jobst A Beiersdorf Co.. The 510(k) number is K963929.

When did JOBST ATHROMBIC PUMP SYSTEM 2100 receive FDA 510(k) clearance?

JOBST ATHROMBIC PUMP SYSTEM 2100 received FDA 510(k) clearance on 1997-01-27, under 510(k) number K963929.

Who is the listed applicant for JOBST ATHROMBIC PUMP SYSTEM 2100?

The FDA 510(k) record lists Jobst A Beiersdorf Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOBST ATHROMBIC PUMP SYSTEM 2100?

The FDA product code for JOBST ATHROMBIC PUMP SYSTEM 2100 is JOW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Jobst A Beiersdorf Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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